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On following pages: 22. New Guinea Sheath-tailed Bat (Emballonura furati); 23. Beccari's Sheath-tailed Bat (Emballonura beccarti); 24. Large-eared Sheath-tailed Bat (Emballonura dianae); 25. Seri'sSheath-tailed Bat (Emballonura sertii); 26. Pacific Sheath-tailed Bat (Emballonura semicaudata); 27. Western Sheath-tailed Bat (Paremballonura tiavato); 28. Peters's Sheath-tailed Bat (Paremballonura atrata); 29. African Sheath-tailed Bat (Coleura afra); 30. Seychelles Sheath-tailed Bat (Coleura seychellensis); 31. Madagascar Sheath-tailed Bat (Coleura kibomalandy); 32. Dark Sheath-tailed Bat (Mosia nigrescens); 33. Chestnut Sac-winged Bat (Cormura brevirostris); 34. Gray Sac-winged Bat (Balantiopteryx plicata); 35. Thomas's Sac-winged Bat (Balantiopteryx io); 36. Ecuadorian Sac-winged Bat (Balantiopteryx infusca). in Emballonuridae
On following pages: 22. New Guinea Sheath-tailed Bat (Emballonura furati); 23. Beccari's Sheath-tailed Bat (Emballonura beccarti); 24. Large-eared Sheath-tailed Bat (Emballonura dianae); 25. Seri'sSheath-tailed Bat (Emballonura sertii); 26. Pacific Sheath-tailed Bat (Emballonura semicaudata); 27. Western Sheath-tailed Bat (Paremballonura tiavato); 28. Peters's Sheath-tailed Bat (Paremballonura atrata); 29. African Sheath-tailed Bat (Coleura afra); 30. Seychelles Sheath-tailed Bat (Coleura seychellensis); 31. Madagascar Sheath-tailed Bat (Coleura kibomalandy); 32. Dark Sheath-tailed Bat (Mosia nigrescens); 33. Chestnut Sac-winged Bat (Cormura brevirostris); 34. Gray Sac-winged Bat (Balantiopteryx plicata); 35. Thomas's Sac-winged Bat (Balantiopteryx io); 36. Ecuadorian Sac-winged Bat (Balantiopteryx infusca).
SrTiO3 EDT series
<p>SrTiO3 EDT series</p>
Insect Galls-Host Plants in Biomes Series (Atlantic Forest) v1.0.3
<p>Insect Galls-Host Plants in Biomes Series (Atlantic Forest) v1.0.3</p>
Figure 6 in An assessment of the status of Polycirridae genera (Annelida: Terebelliformia) and evolutionary transformation series of characters within the family
Figure 6. Amaeana apheles (holotype AM W5239): A, buccal tentacles. Amaeana trilobata (AM W7050): B, C, notopodia, arrows point to nephridial/genital papillae. Polycirrus nonatoi (paratype, MZUSP 1243): D, notopodia, arrows point to cirriform process of postchaetal lobe; E, detail of notochaete. Polycirrus papillosus (paratype, MZUSP 1244): F, notopodium, arrow points to postchaetal lobe. Lysilla bilobata (AM W199514): G, notopodia segments 3–6. Lysilla pacifica (AM W199622): H, notopodia segments 5–7. Except for (D) and (F), unspecified arrows point to nephridial/genital papillae. Scale bars: A, 0.5 mm; B, G, 0.1 mm; C, 40 μm; D, 60 μm; E, 7 μm; F, 50 μm; H, 15 μm.
Figure 9 in An assessment of the status of Polycirridae genera (Annelida: Terebelliformia) and evolutionary transformation series of characters within the family
Figure 9. Biremis blandi (holotype, USNM 47976): A, B, neuropodia from anterior and posterior body, respectively. Amaeana apheles (C, E, AM W10864; D, AM W5384): neuropodia and neurochaetae. Amaeana sp. Brazil (MZUSP 2349): F, neurochaeta. Polycirrus "clavatus" (MZUSP 1246): G, posterior neuropodia; L, uncini from posterior neuropodium. Rhinothelepus occabus (paratype, AM W201904): H, neuropodia from region after notopodia terminate. Amaeana trilobata (neotype, ZMO C3207- 8): I, neurochaetae from segment 45. Polycirrus breviuncinatus (paratype, MZUSP 1245): J, uncinus from posterior neuropodium. Polycirrus bicrinalis (paratype, AM W199638): K, uncini from posterior neuropodium. Polycirrus disjunctus (paratype, AM W199633): M, uncinus from region after notopodia terminate; b, base; h, heel; n, neck; p, prow. Unspecified arrows point to dorsal buttons. Scale bars: A, 2 mm; B, 4 mm; C, 100 μm; D, 20 μm; E, H, 200 μm; F, 2 μm; G, 30 μm; I, L, 10 μm; J–K, 5 μm; M, 7 μm.
Extraction of periodic signals in GNSS vertical coordinate time series using adaptive Ensemble Empirical Modal Decomposition method
Open the record for dataset details and reuse information.
FIGURE 1 in Deciphering a hundred-year-old puzzle: the type series of Bryconamericus exodon (Characiformes: Characidae)
FIGURE 1. Card with curatorial notes on the type series of Bryconamericus exodon after being moved from the Indiana University to the California Academy of Sciences.
FIGURE 5 in A new species of Ischnocnema (Anura: Brachycephalidae) from the mountainous region of Atlantic Forest, southeastern Brazil, with a new phylogeny and diagnose for Ischnocnema parva series
FIGURE 5. Dorsal and ventral color patterns of Ischnocnema crassa sp. nov. paratypes in preservative: (A) adult female MNRJ 93651; (B) adult male MNRJ 93652; (C) adult female MNRJ 93653; (D) adult male MNRJ 93650; (E) adult male MNRJ 93648; and (F) subadult female MBML 11848.
FIGURE 3 in A new species of Ischnocnema (Anura: Brachycephalidae) from the mountainous region of Atlantic Forest, southeastern Brazil, with a new phylogeny and diagnose for Ischnocnema parva series
FIGURE 3. Ischnocnema crassa sp. nov., holotype, adult male (MNRJ 93647): dorsal and lateral views of head; ventral views of right hand, and left foot. Measurements: HL 6.1 mm; HW 7.2 mm; HAL 4.1; FL 8.5.
Figure 17 Bivariate scatterplots showing the relationship between size with maturity among 15 in A high-resolution growth series of Tyrannosaurus rex obtained from multiple lines of evidence
Figure 17 Bivariate scatterplots showing the relationship between size with maturity among 15 specimens of Tyrannosaurus rex. The comparison is limited to specimens that have comparable size data; growth stages (x-axis) and size (y-axis) have been converted to ranks. See Table 15 for the raw data. Full-size DOI: 10.7717/peerj.9192/fig-17
Figure 14 Bivariate scatterplot showing the relationship between maxillary tooth count with maturity among 14 in A high-resolution growth series of Tyrannosaurus rex obtained from multiple lines of evidence
Figure 14 Bivariate scatterplot showing the relationship between maxillary tooth count with maturity among 14 specimens of Tyrannosaurus rex. Growth rank increases away from the origin (i.e., maturity increases to the right) and corresponds to growth stages for which maxillary tooth count was available for a given specimen; that is, the rank does not correspond to growth stage. Maxillary tooth rank corresponds to relative tooth count, where low ranks correspond to high tooth counts and low ranks correspond to high tooth counts. Full-size DOI: 10.7717/peerj.9192/fig-14
Figure 13 in A high-resolution growth series of Tyrannosaurus rex obtained from multiple lines of evidence
Figure 13 Scatterplot showing the congruence in Tyrannosaurus rex between bite force (i.e., and maturity). Growth stage rank, corresponding to the increasing sequence of nodes in Fig. 2, is along the x-axis; growth stage rank refers to the relative maturity of the specimens for which bite force has been estimated. Increasing bite force rank is along the y-axis; raw bite force data are from Bates & Falkingham (2012) and Gignac & Erickson (2017). A Spearman correlation test on these data resulted in a significant correlation coefficient, indicating that bite force increases with maturity. Full-size DOI: 10.7717/peerj.9192/fig-13
Figure 6 in A high-resolution growth series of Tyrannosaurus rex obtained from multiple lines of evidence
Figure 6 Comparison of the frequency distributions of cranial and postcranial changes in the growth series of Tyrannosaurus rex. The growth stages are along the x-axis (corresponding to the numbered nodes of the ontogram in Fig. 2) and the y-axis corresponds to the number of synontomorphies. Cranial changes are shown in solid bars; postcranial chanages are shown in hollow bars. Cranial and postcranial changes tend to follow the same overall pattern although postcranial changes are exceeded by cranial changes, except at growth stages 7, 15, and 16. The relatively late occurrence of postcranial changes (at growth stage 6) is an artifact of the absence of postcranial material among the least mature specimens in the sample. Full-size DOI: 10.7717/peerj.9192/fig-6
Merkel Cell Carcinoma: Evaluation of the Clinico-Pathological Characteristics, Treatment Strategies and Prognostic Factors in a Monocentric Retrospective Series (n=143)
<p><strong>Background: </strong> Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin. The incidence of the disease has undergone a significant increase in recent years, which is caused by an increase in the average age of the population and in the use of immunosuppressive therapies. MCC is an aggressive pathology, which metastasizes early to the lymph nodes. These characteristics impose an accurate diagnostic analysis of the regional lymph node district with radiography, clinical examination and sentinel node biopsy. In recent years, there has been a breakthrough in the treatment of the advanced pathology thanks to the introduction of monoclonal antibodies acting on the PD-1/PD-L1 axis. This study aimed to describe the clinico-pathological characteristics, treatment strategies and prognostic factors of MCC.</p> <p><strong>Methods: </strong> A retrospective cohort study was conducted involving 143 consecutive patients who were diagnosed and/or treated for MCC. These patients were referred to the Veneto Institute of Oncology IOV-IRCCS and to the University Hospital of Padua (a third-level center) in the period between December 1991 and January 2020. In the majority of cases, diagnosis took place at the IOV. However, some patients were diagnosed elsewhere and subsequently referred to the IOV for a review of the diagnosis or to begin specific therapeutic regimens.</p> <p><strong>Results: </strong> 143 patients, with an average age of 71 years, were affected mainly with autoimmune and neoplastic comorbidities. Our analysis has shown that age, autoimmune comorbidities and the use of therapy with immunomodulating drugs (which include corticosteroids, statins and beta-blockers) are associated with a negative prognosis. In this sense, male sex is also a negative prognostic factor.</p> <p><strong>Conclusions: </strong> Autoimmune and neoplastic comorbidities were frequent in the studied population. The use of drugs with immunomodulatory effects was also found to be a common feature of the population under examination. The use of this type of medication is considered a negative prognostic factor. The relevance of a multidisciplinary approach to the patient with MCC is confirmed, with the aim of assessing the risks and benefits related to the use of immunomodulating therapy in the individual patient.</p>
Area averaged Sentinel 2 vegetation Indices time series on NBS and control sites (Panaro River). Further details can be found in D4.5 of the OPERANDUM project.
<p>NBS interventions in OAL-IT (Panaro) aimed at the establishment of a dense deep rooted perennial vegetation on river embankments with the goal to improve the strength of the vadose zone and to reduce erosivity of the soil cover. Monitoring the vegetation cover at the NBS location over time shall provide information about vegetation growth and structure past the completion of the intervention and could give useful insights on the status and effectiveness of the NBS.</p> <p>Dataset includes area averaged Vegetation Indices calculated by a time series of Sentinel-2 multispectral data (10-20 m spatial resolution). Normalized Difference Vegetation Index, Inverted Red-Edge Chlorophyll Index and Red Position Index were calculated for the cloud free images available in the time period between January 2019 and December 2021 providing a total of 71 images covering the NBS site and a control site close to it. The analysis was focused on the evaluation of the temporal profile of Vegetation Indices that can provide metrics of the vigor and health of the vegetation in both the NSB and the standard vegetation (control area).</p>
Serie draverijen
<u>Source</u>: Europeana <br><u>4DCity URL</u>: <a href="https://4dcity.org/imgupload/1652523791.2096.jpg">https://4dcity.org/imgupload/1652523791.2096.jpg</a> <br><u>Original Image URL</u>: <a href="https://api.europeana.eu/thumbnail/v2/url.json?uri=https%3A%2F%2Fwww.openbeelden.nl%2Fimages%2F1271425%2FSerie_draverijen_%25280_44%2529.png&type=VIDEO">https://api.europeana.eu/thumbnail/v2/url.json?uri=https%3A%2F%2Fwww.openbeelden.nl%2Fimages%2F1271425%2FSerie_draverijen_%25280_44%2529.png&type=VIDEO</a> <br><br><u>Image-Metadata:</u><br>Filename: 1652523791.2096.jpg<br>Image Dimensions: 360x288<br>Megapixels: 0.10 MP<br>Filesize: 76.08 KB<br>
Parte de la serie "calles de Bolivia y Perú"
<u>Source</u>: Flickr <br><u>4DCity URL</u>: <a href="https://4dcity.org/imgupload/1665336859.2164.jpg">https://4dcity.org/imgupload/1665336859.2164.jpg</a> <br><u>Original Image URL</u>: <a href="https://live.staticflickr.com/4183/33621253833_8335727515_m.jpg">https://live.staticflickr.com/4183/33621253833_8335727515_m.jpg</a> <br><br><u>Image-Metadata:</u><br>Filename: 1665336859.2164.jpg<br>Image Dimensions: 240x160<br>Megapixels: 0.04 MP<br>Filesize: 20.08 KB<br><br>ExifOffset: 26
Survey of India. STATUS OF 1:50,000 OPEN SERIES MAPS
<p>Survey of India. STATUS OF 1:50,000 OPEN SERIES MAPS.</p>
FIGURE 21 in Towards a Monophyletic Infrageneric Circumscription of Adesmia DC. (Dalbergieae, Leguminosae): a Taxonomic Revision in Adesmia series Adesmia
FIGURE 21. Geographical distribution of Adesmia miottoae Cobra, Iganci & Fort.-Perez, A. muricata (Jacq.) DC., and A. neuquenensis Burkart.
FIGURE 20. A–C in Towards a Monophyletic Infrageneric Circumscription of Adesmia DC. (Dalbergieae, Leguminosae): a Taxonomic Revision in Adesmia series Adesmia
FIGURE 20. A–C. Adesmia punctata (Poir.) DC. D–F. Adesmia miottoae Cobra, Iganci & Fort.-Perez. G–I. Adesmia riograndensis Miotto. J–M. Adesmia securigerifolia Herter. N–P. Adesmia muricata (Jacq.) DC. A. Pedicel of rare axillary flower; narrow-triangular stipules. B. Detail of branch showing long glandular trichomes, with secretion at their tip. C. Hemicraspedium. D. Detail of the calyx indumentum; short glandular trichomes intermixed with adpressed tector trichomes. E. Calyx opened out, inner surface; lobes longer than the tube. F. Hemicraspedium; calyx persistent with lobes twice as long as the tube. G. Paripinnate leaf with six pairs of opposite leaflets. H. Leaflet with a retuse apex. I. Long-pedicellate fruit; muriculate with stiff glandular trichomes. J. Solitary flower from a leaf axil; deltate stipules; calyx lobes shorter than the tube. K. Detail of the calyx indumentum; long glandular trichomes and short tector trichomes adpressed. L. Long-pedicellate lomentum, muriculate with stiff glandular trichomes. M. Reniform seed, without aril. N. Paripinnate leaf with eight pairs of opposite leaflets. O. Orbicular leaflet with retuse apex. P. Long-pedicellate hemicraspedium, with eight muriculate articles. (Illustration: Klei Souza; Vouchers: A–C: Bastos, N. R. s/n; D–F: Valls, J. F. M. et al. 10812; G–I: Valls, J. F. M. et al. 11930; J–M: Bastos, N. R. s/n; N–P: Valls, J. F. M. et al. 10289).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.